نتایج جستجو برای: niemann

تعداد نتایج: 2304  

Journal: :CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2010
Donalee Moulton

2018
Glenn Patriquin Michael Drebot Teri Cole Robbin Lindsay Emily Schleihauf B. Lynn Johnston Kristina Dimitrova Maya Traykova-Andonova Angela Mask David Haldane Todd F. Hatchette

Using residual serum samples from Nova Scotia, Canada, we found that 87.8% of tested deer and an estimated 20.6% of the human population were infected with Jamestown Canyon virus. Human seropositivity reached 48.2% in 1 region. This virus may be an underrecognized cause of disease in Nova Scotia.

Journal: :Journal of Evolution of Medical and Dental Sciences 2012

Journal: :Archives of Disease in Childhood 1970

Journal: :Science translational medicine 2016
Thomas Kirkegaard James Gray David A Priestman Kerri-Lee Wallom Jennifer Atkins Ole Dines Olsen Alexander Klein Svetlana Drndarski Nikolaj H T Petersen Linda Ingemann David A Smith Lauren Morris Claus Bornæs Signe Humle Jørgensen Ian Williams Anders Hinsby Christoph Arenz David Begley Marja Jäättelä Frances M Platt

Lysosomal storage diseases (LSDs) often manifest with severe systemic and central nervous system (CNS) symptoms. The existing treatment options are limited and have no or only modest efficacy against neurological manifestations of disease. We demonstrate that recombinant human heat shock protein 70 (HSP70) improves the binding of several sphingolipid-degrading enzymes to their essential cofacto...

Journal: :Nihon rinsho. Japanese journal of clinical medicine 1995
D D Milovanovitsh A Janeva V Jovanovitsh

A 15-year old girl with slowly progressive gait and speech disorders, and with impairment of mental ability, is decsribed. The disease appeared 18 months before the first hospitalization at the Department of Neurology and Physchiatry for Children and Young People. Neurological and other examinations confirmed extrapyramidal and cerebellar signs, conspisuous knee and ankle reflexes, marked splen...

Journal: :Cell 1995
Bernd Otterbach Wilhelm Stoffel

We have generated an acid sphingomyelinase (aSMase)-deficient mouse line by gene targeting. This novel strain of mutant mouse mimics the lethal, neurovisceral form of the human sphingomyelin storage disease, known as Niemann-Pick disease. Homozygous mice accumulate sphingomyelin extensively in the reticuloendothelial system of liver, spleen, bone marrow, and lung, and in the brain. Most strikin...

Journal: :The Journal of biological chemistry 2010
Katrin Strauss Cornelia Goebel Heiko Runz Wiebke Möbius Sievert Weiss Ivo Feussner Mikael Simons Anja Schneider

Niemann-Pick type C1 disease is an autosomal-recessive lysosomal storage disorder. Loss of function of the npc1 gene leads to abnormal accumulation of free cholesterol and sphingolipids within the late endosomal and lysosomal compartments resulting in progressive neurodegeneration and dysmyelination. Here, we show that oligodendroglial cells secrete cholesterol by exosomes when challenged with ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2016
Xiaochun Li Jiawei Wang Elias Coutavas Hang Shi Qi Hao Günter Blobel

Niemann-Pick C1 protein (NPC1) is a late-endosomal membrane protein involved in trafficking of LDL-derived cholesterol, Niemann-Pick disease type C, and Ebola virus infection. NPC1 contains 13 transmembrane segments (TMs), five of which are thought to represent a "sterol-sensing domain" (SSD). Although present also in other key regulatory proteins of cholesterol biosynthesis, uptake, and signal...

Journal: :Pediatric Neurology Briefs 2012

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